APOL1 polymorphisms are not influencing acute coronary syndrome risk in Czech males

Author:

Hubacek Jaroslav A.12ORCID,Adamkova Vera3,Lanska Vera4,Stanek Vladimir5,Mrazkova Jolana1,Gebauerova Marie5,Kettner Jiri5,Kautzner Josef5,Pitha Jan1

Affiliation:

1. Experimental Medicine Centre Institute for Clinical and Experimental Medicine Prague Czech Republic

2. 3rd Department of Internal Medicine, 1st Faculty of Medicine Charles University Prague Czech Republic

3. Preventive Cardiology Centre Institute for Clinical and Experimental Medicine Prague Czech Republic

4. Department of Informatics Institute for Clinical and Experimental Medicine Prague Czech Republic

5. Cardiology Department Institute for Clinical and Experimental Medicine Prague Czech Republic

Abstract

AbstractBackgroundThe highest mortality and morbidity worldwide is associated with atherosclerotic cardiovascular disease (ASCVD), which has in background both environmental and genetic risk factors. Apolipoprotein L1 (APOL1) variability influences the risk of ASCVD in Africans, but little is known about the APOL1 and ASCVD in other ethnic groups.MethodsTo investigate the role of APOL1 and ASCVD, we have genotyped four (rs13056427, rs136147, rs10854688 and rs9610473) APOL1 polymorphisms in a group of 1541 male patients with acute coronary syndrome (ACS) and 1338 male controls.ResultsIndividual APOL1 polymorphisms were not associated with traditional CVD risk factors such as smoking, hypertension or diabetes prevalence, with BMI values or plasma lipid levels. Neither individual polymorphisms nor haplotypes were associated with an increased risk of ACS nor did they predict total or cardiovascular mortality over the 10.2 ± 3.9 years of follow‐up.ConclusionsWe conclude that APOL1 genetic variability has no major effect on risk of ACS in Caucasians.

Funder

Ministerstvo Zdravotnictví Ceské Republiky

Publisher

Wiley

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